ES2231509T3 - Mezclas herbicidas sinergicas. - Google Patents
Mezclas herbicidas sinergicas.Info
- Publication number
- ES2231509T3 ES2231509T3 ES01943220T ES01943220T ES2231509T3 ES 2231509 T3 ES2231509 T3 ES 2231509T3 ES 01943220 T ES01943220 T ES 01943220T ES 01943220 T ES01943220 T ES 01943220T ES 2231509 T3 ES2231509 T3 ES 2231509T3
- Authority
- ES
- Spain
- Prior art keywords
- ethyl
- cinidon
- phenoxypyrid
- ylcarboxamide
- picolinafen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 75
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 38
- 239000004009 herbicide Substances 0.000 title claims description 10
- 230000002195 synergetic effect Effects 0.000 title description 8
- NNKKTZOEKDFTBU-YBEGLDIGSA-N cinidon ethyl Chemical compound C1=C(Cl)C(/C=C(\Cl)C(=O)OCC)=CC(N2C(C3=C(CCCC3)C2=O)=O)=C1 NNKKTZOEKDFTBU-YBEGLDIGSA-N 0.000 claims abstract description 33
- KWDRLXVLLJFUNF-UHFFFAOYSA-N 6-phenoxypyridine-2-carboxamide Chemical compound NC(=O)C1=CC=CC(OC=2C=CC=CC=2)=N1 KWDRLXVLLJFUNF-UHFFFAOYSA-N 0.000 claims abstract description 19
- -1 cyano, carboxy Chemical group 0.000 claims abstract description 19
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 14
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 10
- 125000004414 alkyl thio group Chemical group 0.000 claims abstract description 9
- 125000001188 haloalkyl group Chemical group 0.000 claims abstract description 7
- 125000005843 halogen group Chemical group 0.000 claims abstract description 7
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 7
- 125000004438 haloalkoxy group Chemical group 0.000 claims abstract description 6
- 125000004995 haloalkylthio group Chemical group 0.000 claims abstract description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 5
- 125000005108 alkenylthio group Chemical group 0.000 claims abstract description 4
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 4
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims abstract description 4
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims abstract description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims abstract description 4
- 125000000547 substituted alkyl group Chemical group 0.000 claims abstract description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 3
- 125000003302 alkenyloxy group Chemical group 0.000 claims abstract description 3
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims abstract description 3
- 125000003368 amide group Chemical group 0.000 claims abstract description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
- 239000001257 hydrogen Substances 0.000 claims abstract description 3
- 241000196324 Embryophyta Species 0.000 claims description 35
- 238000000034 method Methods 0.000 claims description 34
- CWKFPEBMTGKLKX-UHFFFAOYSA-N picolinafen Chemical compound C1=CC(F)=CC=C1NC(=O)C1=CC=CC(OC=2C=C(C=CC=2)C(F)(F)F)=N1 CWKFPEBMTGKLKX-UHFFFAOYSA-N 0.000 claims description 24
- 239000005596 Picolinafen Substances 0.000 claims description 22
- 239000004094 surface-active agent Substances 0.000 claims description 15
- 238000009472 formulation Methods 0.000 claims description 14
- 235000013339 cereals Nutrition 0.000 claims description 11
- 125000004429 atom Chemical group 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 235000021307 Triticum Nutrition 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- 235000008216 herbs Nutrition 0.000 claims description 4
- 241001621841 Alopecurus myosuroides Species 0.000 claims description 3
- 235000009193 Lamium purpureum Nutrition 0.000 claims description 3
- 240000006503 Lamium purpureum Species 0.000 claims description 3
- 240000003461 Setaria viridis Species 0.000 claims description 3
- 235000002248 Setaria viridis Nutrition 0.000 claims description 3
- 240000006694 Stellaria media Species 0.000 claims description 3
- 125000005109 alkynylthio group Chemical group 0.000 claims description 3
- 241001666377 Apera Species 0.000 claims description 2
- 235000014820 Galium aparine Nutrition 0.000 claims description 2
- 240000005702 Galium aparine Species 0.000 claims description 2
- 240000007594 Oryza sativa Species 0.000 claims description 2
- 235000007164 Oryza sativa Nutrition 0.000 claims description 2
- 241000990144 Veronica persica Species 0.000 claims description 2
- 240000008042 Zea mays Species 0.000 claims description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 2
- 235000005822 corn Nutrition 0.000 claims description 2
- 235000009566 rice Nutrition 0.000 claims description 2
- PBBQMDMTGFXPCR-UHFFFAOYSA-N C=1C=CC=NC=1C(=O)NOC1=CC=CC=C1 Chemical compound C=1C=CC=NC=1C(=O)NOC1=CC=CC=C1 PBBQMDMTGFXPCR-UHFFFAOYSA-N 0.000 claims 3
- 241000209140 Triticum Species 0.000 claims 2
- 240000004296 Lolium perenne Species 0.000 claims 1
- 210000000056 organ Anatomy 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 description 35
- 150000001875 compounds Chemical class 0.000 description 34
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000000969 carrier Substances 0.000 description 11
- 239000000839 emulsion Substances 0.000 description 11
- 239000000843 powder Substances 0.000 description 11
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- 239000012141 concentrate Substances 0.000 description 10
- 239000008187 granular material Substances 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 9
- 239000002270 dispersing agent Substances 0.000 description 9
- 235000019198 oils Nutrition 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- 230000000694 effects Effects 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- 239000003921 oil Substances 0.000 description 8
- 239000002671 adjuvant Substances 0.000 description 6
- 238000010410 dusting Methods 0.000 description 6
- 239000003995 emulsifying agent Substances 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 239000007921 spray Substances 0.000 description 6
- 239000000654 additive Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000002689 soil Substances 0.000 description 5
- 239000003381 stabilizer Substances 0.000 description 5
- 239000004562 water dispersible granule Substances 0.000 description 5
- 239000005492 Carfentrazone-ethyl Substances 0.000 description 4
- 239000005531 Flufenacet Substances 0.000 description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- MLKCGVHIFJBRCD-UHFFFAOYSA-N ethyl 2-chloro-3-{2-chloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-4-fluorophenyl}propanoate Chemical group C1=C(Cl)C(CC(Cl)C(=O)OCC)=CC(N2C(N(C(F)F)C(C)=N2)=O)=C1F MLKCGVHIFJBRCD-UHFFFAOYSA-N 0.000 description 4
- 235000013312 flour Nutrition 0.000 description 4
- IANUJLZYFUDJIH-UHFFFAOYSA-N flufenacet Chemical compound C=1C=C(F)C=CC=1N(C(C)C)C(=O)COC1=NN=C(C(F)(F)F)S1 IANUJLZYFUDJIH-UHFFFAOYSA-N 0.000 description 4
- 239000000575 pesticide Substances 0.000 description 4
- 238000001228 spectrum Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 239000004546 suspension concentrate Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000004909 Moisturizer Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 244000098338 Triticum aestivum Species 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 150000005215 alkyl ethers Chemical class 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 230000004071 biological effect Effects 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 150000002191 fatty alcohols Chemical class 0.000 description 3
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000001333 moisturizer Effects 0.000 description 3
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 3
- 239000006072 paste Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 239000004563 wettable powder Substances 0.000 description 3
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 244000192528 Chrysanthemum parthenium Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 240000005979 Hordeum vulgare Species 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 235000017945 Matricaria Nutrition 0.000 description 2
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 235000007846 Papaver rhoeas Nutrition 0.000 description 2
- 240000004674 Papaver rhoeas Species 0.000 description 2
- 244000292693 Poa annua Species 0.000 description 2
- 241001166549 Veronica hederifolia Species 0.000 description 2
- 230000001464 adherent effect Effects 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 244000038559 crop plants Species 0.000 description 2
- 239000013530 defoamer Substances 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 239000004495 emulsifiable concentrate Substances 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 230000012010 growth Effects 0.000 description 2
- 239000003906 humectant Substances 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 230000002688 persistence Effects 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- QTASTLGMYDHNTR-ZSOIEALJSA-N (Z)-2-chloro-3-[2-chloro-5-(1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)phenyl]prop-2-enoic acid Chemical compound C1=C(Cl)C(/C=C(\Cl)C(=O)O)=CC(N2C(C3=C(CCCC3)C2=O)=O)=C1 QTASTLGMYDHNTR-ZSOIEALJSA-N 0.000 description 1
- LQIAZOCLNBBZQK-UHFFFAOYSA-N 1-(1,2-Diphosphanylethyl)pyrrolidin-2-one Chemical compound PCC(P)N1CCCC1=O LQIAZOCLNBBZQK-UHFFFAOYSA-N 0.000 description 1
- XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
- LMCBYQIBQXKCLN-UHFFFAOYSA-N 2,3-dibutylnaphthalene-1-sulfonic acid;naphthalene Chemical compound C1=CC=CC2=CC=CC=C21.C1=CC=C2C(S(O)(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 LMCBYQIBQXKCLN-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 240000007241 Agrostis stolonifera Species 0.000 description 1
- 241000602336 Anthemis arvensis Species 0.000 description 1
- 244000116566 Aphanes arvensis Species 0.000 description 1
- 235000002083 Aphanes arvensis Nutrition 0.000 description 1
- 241000534456 Arenaria <Aves> Species 0.000 description 1
- 235000009066 Atriplex patula Nutrition 0.000 description 1
- 244000022181 Atriplex patula Species 0.000 description 1
- 235000007319 Avena orientalis Nutrition 0.000 description 1
- 244000075850 Avena orientalis Species 0.000 description 1
- 241000209200 Bromus Species 0.000 description 1
- 101100164160 Caenorhabditis elegans atf-7 gene Proteins 0.000 description 1
- 229910021532 Calcite Inorganic materials 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000011305 Capsella bursa pastoris Nutrition 0.000 description 1
- 240000008867 Capsella bursa-pastoris Species 0.000 description 1
- 235000005940 Centaurea cyanus Nutrition 0.000 description 1
- 240000004385 Centaurea cyanus Species 0.000 description 1
- 241000271942 Cerastes Species 0.000 description 1
- 240000006122 Chenopodium album Species 0.000 description 1
- 235000009344 Chenopodium album Nutrition 0.000 description 1
- 241000132536 Cirsium Species 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical class OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- 235000007351 Eleusine Nutrition 0.000 description 1
- 241000209215 Eleusine Species 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 241000221079 Euphorbia <genus> Species 0.000 description 1
- 241001289540 Fallopia convolvulus Species 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 241001508646 Galeopsis tetrahit Species 0.000 description 1
- 241001101998 Galium Species 0.000 description 1
- 241000004701 Geranium dissectum Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 235000009198 Lamium amplexicaule Nutrition 0.000 description 1
- 244000303225 Lamium amplexicaule Species 0.000 description 1
- 241001492668 Legousia hybrida Species 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 241000209082 Lolium Species 0.000 description 1
- 208000002720 Malnutrition Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 244000234597 Montia perfoliata Species 0.000 description 1
- 235000001851 Montia perfoliata Nutrition 0.000 description 1
- 241001442135 Myosotis arvensis Species 0.000 description 1
- 235000009421 Myristica fragrans Nutrition 0.000 description 1
- 244000270834 Myristica fragrans Species 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- WPPOGHDFAVQKLN-UHFFFAOYSA-N N-Octyl-2-pyrrolidone Chemical compound CCCCCCCCN1CCCC1=O WPPOGHDFAVQKLN-UHFFFAOYSA-N 0.000 description 1
- 240000006928 Persicaria lapathifolia Species 0.000 description 1
- 241000745991 Phalaris Species 0.000 description 1
- 241000257649 Phalaris minor Species 0.000 description 1
- 240000006597 Poa trivialis Species 0.000 description 1
- 235000006386 Polygonum aviculare Nutrition 0.000 description 1
- 244000292697 Polygonum aviculare Species 0.000 description 1
- 235000001855 Portulaca oleracea Nutrition 0.000 description 1
- 244000234609 Portulaca oleracea Species 0.000 description 1
- 244000286177 Raphanus raphanistrum Species 0.000 description 1
- 235000000241 Raphanus raphanistrum Nutrition 0.000 description 1
- 239000004113 Sepiolite Substances 0.000 description 1
- 240000003728 Spergula arvensis Species 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 241000404538 Tripleurospermum maritimum subsp. inodorum Species 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 241000394440 Viola arvensis Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 230000004523 agglutinating effect Effects 0.000 description 1
- 230000009418 agronomic effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 125000005133 alkynyloxy group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- ZRIUUUJAJJNDSS-UHFFFAOYSA-N ammonium phosphates Chemical compound [NH4+].[NH4+].[NH4+].[O-]P([O-])([O-])=O ZRIUUUJAJJNDSS-UHFFFAOYSA-N 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000002528 anti-freeze Effects 0.000 description 1
- 239000007798 antifreeze agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- 235000012216 bentonite Nutrition 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000011278 co-treatment Methods 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 239000007931 coated granule Substances 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- FWFSEYBSWVRWGL-UHFFFAOYSA-N cyclohex-2-enone Chemical compound O=C1CCCC=C1 FWFSEYBSWVRWGL-UHFFFAOYSA-N 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical group CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 1
- 229960002380 dibutyl phthalate Drugs 0.000 description 1
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- PZYDAVFRVJXFHS-UHFFFAOYSA-N n-cyclohexyl-2-pyrrolidone Chemical compound O=C1CCCN1C1CCCCC1 PZYDAVFRVJXFHS-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000010742 number 1 fuel oil Substances 0.000 description 1
- 239000001702 nutmeg Substances 0.000 description 1
- 235000018343 nutrient deficiency Nutrition 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- RCMHUQGSSVZPDG-UHFFFAOYSA-N phenoxybenzene;phosphoric acid Chemical compound OP(O)(O)=O.C=1C=CC=CC=1OC1=CC=CC=C1 RCMHUQGSSVZPDG-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000010773 plant oil Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 125000005034 trifluormethylthio group Chemical group FC(S*)(F)F 0.000 description 1
- 125000004950 trifluoroalkyl group Chemical group 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US19438300P | 2000-04-04 | 2000-04-04 | |
| US194383P | 2000-04-04 | ||
| US23163100P | 2000-09-11 | 2000-09-11 | |
| US231631P | 2000-09-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2231509T3 true ES2231509T3 (es) | 2005-05-16 |
Family
ID=26889956
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES01943220T Expired - Lifetime ES2231509T3 (es) | 2000-04-04 | 2001-04-04 | Mezclas herbicidas sinergicas. |
| ES04016188T Expired - Lifetime ES2271742T3 (es) | 2000-04-04 | 2001-04-04 | Mezclas herbicidas sinergicas. |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES04016188T Expired - Lifetime ES2271742T3 (es) | 2000-04-04 | 2001-04-04 | Mezclas herbicidas sinergicas. |
Country Status (30)
| Country | Link |
|---|---|
| US (1) | US6645911B2 (cs) |
| EP (2) | EP1267612B1 (cs) |
| JP (1) | JP4749647B2 (cs) |
| KR (2) | KR100732095B1 (cs) |
| CN (2) | CN1679396A (cs) |
| AT (2) | ATE281073T1 (cs) |
| AU (3) | AU6585701A (cs) |
| BG (2) | BG65872B1 (cs) |
| BR (1) | BR0109821A (cs) |
| CA (2) | CA2654705A1 (cs) |
| CZ (1) | CZ20023303A3 (cs) |
| DE (2) | DE60106885T2 (cs) |
| DK (2) | DK1464223T3 (cs) |
| EA (2) | EA005763B1 (cs) |
| ES (2) | ES2231509T3 (cs) |
| GE (1) | GEP20063846B (cs) |
| HR (2) | HRP20020867B1 (cs) |
| HU (1) | HUP0300564A3 (cs) |
| IL (1) | IL151816A (cs) |
| IN (1) | IN2002CH01751A (cs) |
| MX (1) | MXPA02009480A (cs) |
| NZ (1) | NZ521599A (cs) |
| PL (3) | PL204929B1 (cs) |
| PT (1) | PT1267612E (cs) |
| RS (3) | RS20090500A (cs) |
| SI (1) | SI1464223T1 (cs) |
| SK (1) | SK287815B6 (cs) |
| UA (1) | UA75355C2 (cs) |
| WO (1) | WO2001074157A2 (cs) |
| ZA (1) | ZA200208902B (cs) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1351571A2 (de) * | 1999-11-17 | 2003-10-15 | Bayer CropScience AG | Selektive herbizide auf basis von 2,6-disubstituierten pyridin-derivaten |
| DE10160139A1 (de) * | 2001-12-07 | 2003-06-18 | Bayer Cropscience Gmbh | Synergistische herbizide Mittel enthaltend bestimmte Herbizide aus der Gruppe der Benzoylcylohexandione |
| ES2315562T3 (es) * | 2002-08-08 | 2009-04-01 | Syngenta Participations Ag | Composicion herbicida. |
| MXPA05009115A (es) | 2003-03-13 | 2005-10-20 | Basf Ag | Mezclas herbicidas. |
| KR20050114651A (ko) * | 2003-03-13 | 2005-12-06 | 바스프 악티엔게젤샤프트 | 상승작용 제초제 혼합물 |
| WO2006006569A1 (ja) * | 2004-07-12 | 2006-01-19 | Nihon Nohyaku Co., Ltd. | フェニルピリジン類又はその塩類、これらを有効成分とする除草剤及びその使用方法 |
| EP2203865A2 (en) | 2007-09-24 | 2010-07-07 | Apple Inc. | Embedded authentication systems in an electronic device |
| JP5563773B2 (ja) * | 2008-12-17 | 2014-07-30 | バイエル・クロップサイエンス・アーゲー | 除草剤組成物 |
| AR093955A1 (es) * | 2012-12-18 | 2015-07-01 | Bayer Cropscience Ag | Agentes herbicidas que contienen aclonifeno |
| EP2875727A1 (en) * | 2013-11-26 | 2015-05-27 | Basf Se | Aqueous suspension concentrates containing picolinafen |
| WO2015086605A1 (de) * | 2013-12-11 | 2015-06-18 | Bayer Cropscience Ag | Herbizide mittel enthaltend flufenacet, picolinafen und metribuzin |
| WO2015086603A1 (de) * | 2013-12-11 | 2015-06-18 | Bayer Cropscience Ag | Herbizide mittel enthaltend flufenacet, picolinafen und pendimethalin |
| CN113180037B (zh) * | 2020-01-14 | 2024-02-02 | 东莞市东阳光菌阳氢专利农药有限公司 | 一种环保型氟苯醚酰胺乳油制剂及其制备方法和用途 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3603789A1 (de) | 1986-02-07 | 1987-08-13 | Basf Ag | N-substituierte 3,4,5,6-tetrahydrophthalimide |
| US5237089A (en) | 1986-02-07 | 1993-08-17 | Basf Aktiengesellschaft | Nitro or amino substituted phenylalkyl or phenylalkenyl carboxylic acid derivatives |
| DE3821600A1 (de) * | 1988-06-27 | 1989-12-28 | Bayer Ag | Heteroaryloxyessigsaeure-n-isopropylanilide |
| GB9005965D0 (en) * | 1990-03-16 | 1990-05-09 | Shell Int Research | Herbicidal carboxamide derivatives |
| CN1074646C (zh) * | 1992-10-06 | 2001-11-14 | 国际壳牌研究有限公司 | 除草剂混合物 |
| DE19534910A1 (de) | 1995-09-20 | 1997-03-27 | Basf Ag | Herbizide Mischungen mit synergistischer Wirkung |
| US5859920A (en) * | 1995-11-30 | 1999-01-12 | Eastman Kodak Company | Method for embedding digital information in an image |
| DE19633271A1 (de) * | 1996-08-19 | 1998-02-26 | Basf Ag | Flüssige Formulierung von Ethyl-(Z)-2-chlor-3-[2-chlor-5-(4,5,6,7-tetrahydro-1,3-dioxoisoindoldion-2-yl)phenyl]acrylat |
| US6030924A (en) * | 1997-05-07 | 2000-02-29 | American Cyanamid Company | Solid formulations |
| JPH11116408A (ja) * | 1997-10-07 | 1999-04-27 | Sumitomo Chem Co Ltd | 除草剤組成物 |
| US5985796A (en) * | 1998-01-22 | 1999-11-16 | American Cyanamid Company | Herbicidal mixtures |
| JP2000038307A (ja) * | 1998-07-23 | 2000-02-08 | Sumitomo Chem Co Ltd | 除草剤組成物 |
| WO2000007447A1 (fr) * | 1998-08-07 | 2000-02-17 | Sumitomo Chemical Company, Limited | Composition herbicide |
| US6486096B1 (en) | 1998-08-13 | 2002-11-26 | Hoechst Schering Agrevo Gmbh | Herbicidal compositions with acylated aminophenylsulfonylureas |
| DE19836700A1 (de) * | 1998-08-13 | 2000-02-17 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel für tolerante oder resistente Getreidekulturen |
| EP1221848B1 (de) * | 1999-09-30 | 2006-01-25 | Bayer CropScience AG | Selektive herbizide auf basis eines n-aryl-triazolinons |
| US6252336B1 (en) * | 1999-11-08 | 2001-06-26 | Cts Corporation | Combined piezoelectric silent alarm/battery charger |
| EP1351571A2 (de) * | 1999-11-17 | 2003-10-15 | Bayer CropScience AG | Selektive herbizide auf basis von 2,6-disubstituierten pyridin-derivaten |
-
2001
- 2001-04-04 MX MXPA02009480A patent/MXPA02009480A/es active IP Right Grant
- 2001-04-04 PL PL360851A patent/PL204929B1/pl unknown
- 2001-04-04 RS RSP-2009/0500A patent/RS20090500A/sr unknown
- 2001-04-04 DK DK04016188T patent/DK1464223T3/da active
- 2001-04-04 RS YU73602A patent/RS51691B/sr unknown
- 2001-04-04 WO PCT/EP2001/003833 patent/WO2001074157A2/en active Application Filing
- 2001-04-04 PL PL384851A patent/PL204904B1/pl not_active IP Right Cessation
- 2001-04-04 EA EA200201051A patent/EA005763B1/ru not_active IP Right Cessation
- 2001-04-04 SK SK1425-2002A patent/SK287815B6/sk not_active IP Right Cessation
- 2001-04-04 CA CA002654705A patent/CA2654705A1/en not_active Abandoned
- 2001-04-04 EP EP01943220A patent/EP1267612B1/en not_active Expired - Lifetime
- 2001-04-04 GE GE4971A patent/GEP20063846B/en unknown
- 2001-04-04 DK DK01943220T patent/DK1267612T3/da active
- 2001-04-04 RS RSP-2009/0499A patent/RS20090499A/sr unknown
- 2001-04-04 CZ CZ20023303A patent/CZ20023303A3/cs unknown
- 2001-04-04 JP JP2001571921A patent/JP4749647B2/ja not_active Expired - Fee Related
- 2001-04-04 EP EP04016188A patent/EP1464223B1/en not_active Expired - Lifetime
- 2001-04-04 AU AU6585701D patent/AU6585701A/xx active Pending
- 2001-04-04 BR BR0109821-7A patent/BR0109821A/pt not_active Application Discontinuation
- 2001-04-04 AT AT01943220T patent/ATE281073T1/de not_active IP Right Cessation
- 2001-04-04 DE DE60106885T patent/DE60106885T2/de not_active Expired - Fee Related
- 2001-04-04 AT AT04016188T patent/ATE336895T1/de not_active IP Right Cessation
- 2001-04-04 ES ES01943220T patent/ES2231509T3/es not_active Expired - Lifetime
- 2001-04-04 EA EA200400926A patent/EA006848B1/ru not_active IP Right Cessation
- 2001-04-04 AU AU2001265857A patent/AU2001265857B2/en not_active Ceased
- 2001-04-04 US US09/825,694 patent/US6645911B2/en not_active Expired - Fee Related
- 2001-04-04 PL PL384852A patent/PL204905B1/pl not_active IP Right Cessation
- 2001-04-04 KR KR1020027013215A patent/KR100732095B1/ko not_active IP Right Cessation
- 2001-04-04 DE DE60122600T patent/DE60122600T2/de not_active Expired - Fee Related
- 2001-04-04 SI SI200130610T patent/SI1464223T1/sl unknown
- 2001-04-04 PT PT01943220T patent/PT1267612E/pt unknown
- 2001-04-04 CA CA002404353A patent/CA2404353A1/en not_active Abandoned
- 2001-04-04 CN CNA2005100694761A patent/CN1679396A/zh active Pending
- 2001-04-04 IL IL151816A patent/IL151816A/en active IP Right Grant
- 2001-04-04 NZ NZ521599A patent/NZ521599A/en not_active IP Right Cessation
- 2001-04-04 CN CNB018074944A patent/CN1220433C/zh not_active Expired - Fee Related
- 2001-04-04 ES ES04016188T patent/ES2271742T3/es not_active Expired - Lifetime
- 2001-04-04 UA UA2002118717A patent/UA75355C2/uk unknown
- 2001-04-04 KR KR1020077009449A patent/KR100736312B1/ko not_active IP Right Cessation
- 2001-04-04 HU HU0300564A patent/HUP0300564A3/hu unknown
-
2002
- 2002-09-30 BG BG107158A patent/BG65872B1/bg unknown
- 2002-10-24 IN IN1751CH2002 patent/IN2002CH01751A/en unknown
- 2002-11-01 ZA ZA200208902A patent/ZA200208902B/en unknown
- 2002-11-04 HR HR20020867A patent/HRP20020867B1/xx not_active IP Right Cessation
-
2007
- 2007-01-25 AU AU2007200321A patent/AU2007200321B2/en not_active Ceased
-
2008
- 2008-06-30 HR HRP20080308AA patent/HRP20080308B1/hr not_active IP Right Cessation
-
2009
- 2009-09-02 BG BG10110457A patent/BG110457A/bg unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| RU2632968C2 (ru) | Гербицидные композиции, содержащие 4-амино-3-хлор-5-фтор-6-(4-хлор-2-фтор-3-метоксифенил)пиридин-2-карбоновую кислоту или ее производное и синтетические ауксиновые гербициды | |
| AU2007200321B2 (en) | Synergistic Herbicidal Mixtures | |
| JP7015816B2 (ja) | ペノキシスラムおよびベンゾビシクロンまたはクロマゾンおよびベンゾビシクロンの施用からの相乗的雑草防除 | |
| RU2639885C2 (ru) | Гербицидные композиции, содержащие 4-амино-3-хлор-5-фтор-6-(4-хлор-2-фтор-3-метоксифенил)пиридин-2-карбоновую кислоту или ее производное и некоторые ингибиторы ps ii | |
| KR101525558B1 (ko) | 벼농사에 사용되는 벤조일사이클로헥산디온 그룹의 상승적 작물 내성 제초제 배합물 | |
| BR102013018646B1 (pt) | Composições herbicidas compreendendo ácido 4-amino-3-cloro-5-flúor-6-(4-cloro-2-flúor-3-metoxi-fenil) piridina-2-carboxílico ou um derivado do mesmo e triazolopirimidina sulfonamidas, e método para controlar vegetação indesejável | |
| RU2617269C2 (ru) | Гербицидная композиция, содержащая некоторые пиридинкарбоновые кислоты и (2,4-дихлорфенокси)уксусную кислоту | |
| US8865626B2 (en) | Synergistically active herbicidal agents that are compatible with cultivated plants and contain herbicides from the group of benzoylpyrazoles | |
| JP2554501B2 (ja) | ジフルフエニカンを使用する除草方法 | |
| EP0937397B1 (en) | Herbicidal mixtures | |
| AU2001265857A1 (en) | Synergistic herbicidal mixtures |